| Literature DB >> 25044433 |
Paola Galletti1, Matteo Pori, Federica Funiciello, Roberto Soldati, Alberto Ballardini, Daria Giacomini.
Abstract
By combining two green and efficient catalysts, such as the commercially available enzyme laccase from Trametes versicolor and the stable free radical 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO), the oxidation in water of some primary alcohols to the corresponding carboxylic acids or aldehydes and of selected secondary alcohols to ketones can be accomplished. The range of applicability of bio-oxidation is widened by applying the optimized protocol to the oxidation of enantiomerically pure 2-arylpropanols (profenols) into the corresponding 2-arylpropionic acids (profens), in high yields and with complete retention of configuration.Entities:
Keywords: alcohols; drug design; enzyme catalysis; oxidation; selectivity
Mesh:
Substances:
Year: 2014 PMID: 25044433 DOI: 10.1002/cssc.201402136
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928